© 2012 AOAC INTERNATIONAL
G
UIDELINES
FOR
S
TANDARD
M
ETHOD
P
ERFORMANCE
R
EQUIREMENTS
AOAC O
FFICIAL
M
ETHODS
OF
A
NALYSIS
(2012)
Appendix F, p. 4
For projects with multiple analytes, for example, vitamins A, D,
E, and K in infant formula, it may be useful to organize a separate
working group to fully describe the matrix(es) so that a common
description of the matrix(es) can be applied to all of the analytes.
For single analyte SMPRs, it is most common to organize the
method performance requirements into a table with 2–3 columns
as illustrated in Table 1. For multiple analyte SMPRs, it is often
convenient to present the requirements in an expanded table with
analytes forming additional columns as illustrated in Table 2.
Once the intended use, analytical techniques, and method
performance requirements have been determined, then a working
group can proceed to consider the quality control parameters,
such as the minimum validation requirements, system suitability
procedures, and reference materials (if available). It is not
uncommon that an appropriate reference material is not available.
Annex F
of the SMPR Guidelines provides comprehensive guidance
for the development and use of in-house reference materials.
Most working groups are able to prepare a consensus SMPR in
about 3 months.
Open Comment Period
Once a working group has produced a draft standard, AOAC
opens a comment period for the standard. The comment period
provides an opportunity for other stakeholders to state their
perspective on the draft SMPR. All collected comments are
reviewed by the AOAC CSO and the working group chair, and the
comments are reconciled. If there are significant changes required
to the draft standard as a result of the comments, the working group
is convened to discuss and any unresolved issues will be presented
for discussion at the stakeholder panel meeting.
Submission of Draft SMPRs to the Stakeholder Panel
Stakeholder panels meet several times a year at various locations.
The working group chair (or designee) presents a draft SMPR to the
stakeholder panel for review and discussion. Aworking group chair
is expected to be able to explain the conclusions of the working
group, discuss comments received, and to answer questions from
the stakeholder panel. The members of the stakeholder panel may
revise, amend, approve, or defer a decision on the proposed SMPR.
A super majority of 2/3 or more of those voting is required to adopt
an SMPR as an AOAC voluntary consensus standard.
Publication
Adopted SMPRs are prepared for publication by AOAC staff,
and are published in the
Journal of AOAC INTERNATIONAL
and in
the AOAC
Official Methods of Analysis
SM
compendium. Often, the
AOAC CSO and working group chair prepare a companion article
to introduce an SMPR and describe the analytical issues considered
and resolved by the SMPR. An SMPR is usually published within
6 months of adoption.
Conclusion
SMPRs are a unique and novel concept for the analytical
methods community. SMPRs are voluntary, consensus standards
developed by stakeholders that prescribe the minimum analytical
performance requirements for classes of analytical methods. The
SMPR Guidelines provide a structure for working groups to use
as they develop an SMPR. The guidelines have been employed in
several AOAC projects and have been proven to be very useful. The
guidelines are not a statute that users must conform to; they are a
“living” document that is regularly updated, so users should check
the AOAC website for the latest version before using the guidelines.
References
(1) Eurachem,
The Fitness for Purpose of Analytical Methods:
A Laboratory Guide to Method Validation and Related
Topics, Validation
,
/
valid.pdf, posted December 1998, accessed March 2012
(2)
Guidelines for Collaborative Study Procedures to
Validate Characteristics of a Method of Analysis
(2012)
Official Methods of Analysis, Appendix D
, AOAC
INTERNATIONAL, Gaithersburg, MD
(3)
AOAC INTERNATIONAL Methods Committee Guidelines
for Validation of Biological Threat Agent Methods and/
or Procedures
(2012)
Official Methods of Analysis,
19th
Ed.,
Appendix I, Calculation of CPOD and dCPOD Values
from Qualitative Method Collaborative Study Data
, AOAC
INTERNATIONAL, Gaithersburg, MD
(4)
AOAC Guidelines for Single-Laboratory Validation of
Chemical Methods for Dietary Supplements and Botanicals
(2012)
Official Methods of Analysis
, 19th Ed.,
Appendix K
,
AOAC INTERNATIONAL, Gaithersburg, MD
(5) Codex Alimentarius Codex Procedure Manual
(6) International Organization for Standardization, Geneva,
Switzlerland
Table 2. Example of method performance table for multiple analytes
Analyte 1
Analyte 2
Analyte 3
Analytical range
10–20 μg/mL
100–200 μg/mL
200–500 μg/mL
Limit of quantitation (LOQ)
10 μg/mL
100 μg/mL
200 μg/mL
Repeatability (RSD
r
)
<10 μg/mL
8%
<10 μg/mL
8%
<200 μg/mL
10%
10 μg/mL
6%
10 μg/mL
6%
200 μg/mL
8%
